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Disease Ontology Browser
familial partial lipodystrophy type 5 (DOID:0070203)
Alliance: disease page
Synonyms: CIDEC-related FPLD; familial partial lipodystrophy associated with CIDEC mutations; FPLD5
Alt IDs: OMIM:615238, ORDO:435651
Definition: A familial partial lipodystrophy characterized by autosomal recessive inheritance that has_material_basis_in mutation in the CIDEC gene on chromosome 3p25.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
02/18/2020
MGI 6.14
The Jackson Laboratory